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M Bamshad

Showing results (41-50 of 47) with videos related to

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Nature Genetics|July 1, 1997
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeM Bamshad, R C Lin, D J Law, et al.
American Journal of Physical Anthropology|June 23, 1999
Multiple origins of the mtDNA 9-bp deletion in populations of South IndiaW S Watkins, M Bamshad, M E Dixon, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
Genome Research|May 31, 2001
Genetic evidence on the origins of Indian caste populationsM Bamshad, T Kivisild, W S Watkins, et al.
Cell|October 27, 1999
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Race-specific HIV-1 disease-modifying effects associated with CCR5 haplotypesE Gonzalez, M Bamshad, N Sato, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Nature Genetics|July 1, 1997
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeM Bamshad, R C Lin, D J Law, et al.
American Journal of Physical Anthropology|June 23, 1999
Multiple origins of the mtDNA 9-bp deletion in populations of South IndiaW S Watkins, M Bamshad, M E Dixon, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
Genome Research|May 31, 2001
Genetic evidence on the origins of Indian caste populationsM Bamshad, T Kivisild, W S Watkins, et al.
Cell|October 27, 1999
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Race-specific HIV-1 disease-modifying effects associated with CCR5 haplotypesE Gonzalez, M Bamshad, N Sato, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
Pageof 5